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Alliance of Genome Resources

Alliance of Genome Resources is a gene dataset, which contains curated genome information essential for the understanding of the genetics and genomic basis of human biology, health and disease. All data is retrieved from six major model organism databases and the Gene Ontology including FlyBase, Mouse Genome Database (MGI), Rat Genome Database (RGD), Saccharomyces Genome Database (SGD), WormBase, Zebrafish Information Network (ZFIN), and the GO Consortium. In GlyCosmos, only glycan-related disease information has been extracted from Alliance of Genome Resources.

Source Last Updated
Alliance of Genome Resources July 29, 2024
Displaying entries 2576 - 2600 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:9452 steatotic liver disease HGNC:16940 Homo sapiens (human) 84649 DGAT2
  • MGI:6194238
DOID:10787 premature menopause HGNC:16940 Homo sapiens (human) 84649 DGAT2
  • MGI:6194238
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:16940 Homo sapiens (human) 84649 DGAT2
  • MGI:6194238
  • PMID:17618857
DOID:332 amyotrophic lateral sclerosis HGNC:17074 Homo sapiens (human) 23098 SARM1
  • MGI:6194238
DOID:1289 neurodegenerative disease HGNC:17074 Homo sapiens (human) 23098 SARM1
  • MGI:6194238
DOID:0080288 spinocerebellar ataxia 46 HGNC:17158 Homo sapiens (human) 23646 PLD3
  • RGD:7240710
DOID:0080379 nephrotic syndrome type 2 HGNC:17175 Homo sapiens (human) 51196 PLCE1
  • PMID:20591883
DOID:0080382 nephrotic syndrome type 3 HGNC:17175 Homo sapiens (human) 51196 PLCE1
  • RGD:7240710
DOID:1184 nephrotic syndrome HGNC:17175 Homo sapiens (human) 51196 PLCE1
  • PMID:17086182
DOID:3717 gastric adenocarcinoma HGNC:17175 Homo sapiens (human) 51196 PLCE1
  • PMID:24796667
DOID:0050814 temtamy preaxial brachydactyly syndrome HGNC:17198 Homo sapiens (human) 22856 CHSY1
  • RGD:7240710
DOID:0060576 3MC syndrome 2 HGNC:17213 Homo sapiens (human) 78989 COLEC11
  • RGD:7240710
DOID:674 cleft palate HGNC:17213 Homo sapiens (human) 78989 COLEC11
  • MGI:6194238
DOID:1094 attention deficit hyperactivity disorder HGNC:17223 Homo sapiens (human) 10090 UST
  • PMID:35642741
DOID:10763 hypertension HGNC:17423 Homo sapiens (human) 55501 CHST12
  • MGI:6194238
DOID:2841 asthma HGNC:17432 Homo sapiens (human) 27159 CHIA
  • PMID:15192232
  • PMID:16179638
  • PMID:20226308
DOID:12053 cryptococcosis HGNC:17432 Homo sapiens (human) 27159 CHIA
  • MGI:6194238
DOID:0050127 sinusitis HGNC:17432 Homo sapiens (human) 27159 CHIA
  • PMID:19379605
DOID:10325 silicosis HGNC:17432 Homo sapiens (human) 27159 CHIA
  • MGI:6194238
DOID:2871 endometrial carcinoma HGNC:1753 Homo sapiens (human) 1012 CDH13
  • PMID:18519763
DOID:2349 arteriosclerosis HGNC:1753 Homo sapiens (human) 1012 CDH13
  • PMID:11326751
DOID:1612 breast cancer HGNC:1753 Homo sapiens (human) 1012 CDH13
  • PMID:17764565
  • PMID:8673923
DOID:3908 lung non-small cell carcinoma HGNC:1753 Homo sapiens (human) 1012 CDH13
  • PMID:11389090
DOID:3459 breast carcinoma HGNC:1753 Homo sapiens (human) 1012 CDH13
  • PMID:11389090
DOID:4362 cervical cancer HGNC:1753 Homo sapiens (human) 1012 CDH13
  • PMID:17548682

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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024